Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands

Introduction Familial hypercholesterolaemia (FH) is the most common monogenic autosomal dominant genetic disorder and is associated with a high risk of premature atherosclerotic cardiovascular disease. The prevalence of FH has been reported to be particularly high in certain founder populations. The...

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Ngā kaituhi matua:	Peter Søgaard, Albert Marni Joensen, Søren Lundbye-Christensen, Erik Berg Schmidt, Jan Jóanesarson, Christian Sørensen Bork, Tomas Zaremba, Sanna á Borg, Michael Rene Skjelbo Nielsen, Rudi Kollslíð
Hōputu:	Artigo
Reo:	Inglês
I whakaputaina:	BMJ Publishing Group 2022-04-01
Rangatū:	BMJ Open
Urunga tuihono:	https://bmjopen.bmj.com/content/12/4/e050857.full
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